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Quality Assurance Documentation Lead: MasterControl & Stability Expert
Job in
South Brunswick, Middlesex County, New Jersey, USA
Listed on 2026-09-09
Listing for:
Tris Pharma, Inc
Full Time
position Listed on 2026-09-09
Job specializations:
-
Quality Assurance - QA/QC
QA Specialist - Analyst/Manager, Quality Control - QC Analysts/Managers, Regulatory Compliance Specialist
Job Description & How to Apply Below
Tris Pharma, Inc. in Monmouth, NJ is seeking a Quality Assurance Documentation Lead to support the QA function and ensure manufacturing quality controls comply with SOPs, cGMPs and FDA standards.
Under QA Mgmt, you will handle day-to-day operational QA activities across multiple departments, maintain GxP records, support Master Control systems, and ensure timely APR sub-reports for resin-based ER tablets and related products. Fluency in English is required. Background checks may be conducted.
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